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采用外固定技术行广泛的中足色素沉着绒毛结节性滑膜炎切除并吻合髂嵴骨移植微血管:1例报告

Excision of extensive midfoot pigmented villonodular synovitis with microvascular anastamosis of iliac crest bone graft using external fixation: a case report.

作者信息

Oloff Lawrence, Miller Kevin

机构信息

Sports, Orthopedics and Rehabilitative Medicine Associates, Redwood City, CA, USA.

出版信息

Foot Ankle Spec. 2011 Oct;4(5):301-5. doi: 10.1177/1938640011412952. Epub 2011 Sep 16.

DOI:10.1177/1938640011412952
PMID:21926367
Abstract

Pigmented villonodular synovitis (PVNS) is a relatively rare lesion in the foot and ankle, most commonly involving the ankle joint and atypically, the subtalar and midtarsal joints. It is a benign proliferative disease characterized by an increase in villous or nodular synovium in joints. Resection of the tumor is often indicated in most cases because of the potentially aggressive joint destructive nature of this lesion. This report presents a case of chronic enlarging pervasive midtarsal and metatarsal-cuneiform joint PVNS in a 28-year-old male. This patient had a midtarsal mass that enlarged over a period of 2 years, causing increased pain, deformity, and difficulty with ambulation. Cross-sectional imaging studies identified evidence of erosive disease through much of the midfoot articulations, with biopsy confirming the mass as PVNS. The dimensions of the mass approximated 5.5 cm × 4.1 cm × 2.8 cm. Simple resection was problematic because of the size and multiple joints involved. Amputation was most commonly advised by multiple consultants. The patient preferred attempt at limb salvage. En bloc resection and placement of a revascularized iliac crest bone graft was used to fill the defect. The graft was microvascularly anastamosed and fixated with standard external fixation. Pathologic and histologic specimens from surgical biopsy reconfirmed the diagnosis of PVNS postoperatively. Second-stage arthrodesis was performed when the patient was stable and disease free. The patient was followed postoperatively for 10 years without recurrence and was able to return to full function and partake in moderate athletic activity at last visit. This case describes a retrospective review of the procedure and reconstruction, as well as an overview of current surgical management of PVNS.

摘要

色素沉着绒毛结节性滑膜炎(PVNS)在足踝部是一种相对罕见的病变,最常累及踝关节,非典型情况下也可累及距下关节和中跗关节。它是一种良性增生性疾病,其特征是关节内绒毛状或结节状滑膜增生。由于该病变具有潜在的侵袭性关节破坏性质,大多数情况下通常需要进行肿瘤切除。本报告介绍了一名28岁男性慢性进行性中跗关节和跖楔关节PVNS的病例。该患者中跗部有一肿物,在2年时间里逐渐增大,导致疼痛加剧、畸形以及行走困难。横断面影像学研究发现中足多个关节存在侵蚀性病变证据,活检证实肿物为PVNS。肿物尺寸约为5.5厘米×4.1厘米×2.8厘米。由于肿物大小及累及多个关节,单纯切除存在问题。多位会诊医生大多建议截肢。患者更倾向于尝试保肢治疗。采用整块切除并植入带血管蒂的髂嵴骨移植来填充缺损。将移植骨进行微血管吻合并用标准外固定器固定。手术活检的病理和组织学标本术后再次证实为PVNS。当患者病情稳定且无疾病时进行了二期关节融合术。术后对患者进行了10年随访,无复发,患者最终恢复了全部功能并能够参加适度的体育活动。本病例描述了对该手术及重建过程的回顾性研究,以及PVNS当前外科治疗的概述。

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